510(k) K920219

KINAMED 26MM BIOCERAN-Z TOTAL HIP FEMORAL BALL by Kinamed, Inc. — Product Code LZO

K920219 is an FDA 510(k) premarket notification submitted by Kinamed, Inc. for the device "KINAMED 26MM BIOCERAN-Z TOTAL HIP FEMORAL BALL". The FDA issued a decision of Substantially Equivalent on October 30, 1992. The device falls under product code LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented), a Class II device regulated under 21 CFR 888.3353. Kinamed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 30, 1992
Date Received
January 16, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Device Class
Class II
Regulation Number
888.3353
Review Panel
OR
Submission Type